MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; BED, SEMI ELECTRIC, MEDLITE

Catalog Number	MDR107002L
Medical Device Problem Code	Electrical /Electronic Property Problem (1198)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/13/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "for both beds all functions of the bed work besides the head/foot section of the bed will not go up or down." customer stated that "the hand remote is not working and all they could hear is a \"humming or clicking noise\" and the bed does not move.".
Additional Manufacturer Narrative
The customer stated they have two beds with the exact same issue; all functions of the bed work besides the head/foot section of the bed will not go up or down, the hand remote is not working, a "humming or clicking noise" could be heard, and the bed does not move.The investigation noted that no sample or photo was available; pcn history was reviewed with no product changes identified that could have contributed to this product failure, and quality control inspection records were reviewed with the product passed inspection per the inspection report.The division will monitor through quarterly trending, and a formal investigation will be conducted should the sample arrive, or if a detailed photo is provided.There were no reports of death, serious injury, medical intervention, or follow up care.It has been determined that the reported event could cause or contribute to serious injury if it were to occur again.In an abundance of caution, this is a reportable event.If additional information becomes available this report will be reopened and reevaluated.This medical device report (mdr) is being submitted as part of retrospective review activities, which include review of historical data in accordance with regulations at 21 cfr part 803.The information included in this mdr reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.

• Brand Name: MEDLINE
• Common Device Name: BED, SEMI ELECTRIC, MEDLITE
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: connor klawikowski ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50873235
• Report Number: 1417592-2026-49432
• Device Sequence Number: 9314228
• Product Code: LLI
• UDI-Device Identifier: 40080196294320
• UDI-Public: 40080196294320
• Combination Product (Y/N): N
• Initial Reporter State: DC
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/16/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: MDR107002L
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/13/2023
• Initial Report FDA Received Date: 09/23/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown